Vibrational transitions in hydrogen bonded bimolecular complexes – A local mode perturbation theory approach to transition frequencies and intensities

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Standard

Vibrational transitions in hydrogen bonded bimolecular complexes – A local mode perturbation theory approach to transition frequencies and intensities. / Mackeprang, Kasper; Kjærgaard, Henrik Grum.

I: Journal of Molecular Spectroscopy, Bind 334, 2017, s. 1-9.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Mackeprang, K & Kjærgaard, HG 2017, 'Vibrational transitions in hydrogen bonded bimolecular complexes – A local mode perturbation theory approach to transition frequencies and intensities', Journal of Molecular Spectroscopy, bind 334, s. 1-9. https://doi.org/10.1016/j.jms.2017.02.005

APA

Mackeprang, K., & Kjærgaard, H. G. (2017). Vibrational transitions in hydrogen bonded bimolecular complexes – A local mode perturbation theory approach to transition frequencies and intensities. Journal of Molecular Spectroscopy, 334, 1-9. https://doi.org/10.1016/j.jms.2017.02.005

Vancouver

Mackeprang K, Kjærgaard HG. Vibrational transitions in hydrogen bonded bimolecular complexes – A local mode perturbation theory approach to transition frequencies and intensities. Journal of Molecular Spectroscopy. 2017;334:1-9. https://doi.org/10.1016/j.jms.2017.02.005

Author

Mackeprang, Kasper ; Kjærgaard, Henrik Grum. / Vibrational transitions in hydrogen bonded bimolecular complexes – A local mode perturbation theory approach to transition frequencies and intensities. I: Journal of Molecular Spectroscopy. 2017 ; Bind 334. s. 1-9.

Bibtex

@article{c48de33645fc40ca879dbfe67dd1cc0b,
title = "Vibrational transitions in hydrogen bonded bimolecular complexes – A local mode perturbation theory approach to transition frequencies and intensities",
abstract = "The local mode perturbation theory (LMPT) model was developed to improve the description of hydrogen bonded XH-stretching transitions, where X is typically O or N. We present a modified version of the LMPT model to extend its application from hydrated bimolecular complexes to hydrogen bonded bimolecular complexes with donors such as alcohols, amines and acids. We have applied the modified model to a series of complexes of different hydrogen bond type and complex energy. We found that the differences between local mode (LM) and LMPT calculated fundamental XH-stretching transition wavenumbers and oscillator strengths were correlated with the strength of the hydrogen bond. Overall, we have found that the LMPT model in most cases predicts transition wavenumbers within 20 cm−1 of the experimental values.",
keywords = "Explicitly correlated coupled cluster, Frequency redshift, Hydrogen bonds, Intensity enhancement, Vibrational spectroscopy",
author = "Kasper Mackeprang and Kj{\ae}rgaard, {Henrik Grum}",
year = "2017",
doi = "10.1016/j.jms.2017.02.005",
language = "English",
volume = "334",
pages = "1--9",
journal = "Journal of Molecular Spectroscopy",
issn = "0022-2852",
publisher = "Academic Press",

}

RIS

TY - JOUR

T1 - Vibrational transitions in hydrogen bonded bimolecular complexes – A local mode perturbation theory approach to transition frequencies and intensities

AU - Mackeprang, Kasper

AU - Kjærgaard, Henrik Grum

PY - 2017

Y1 - 2017

N2 - The local mode perturbation theory (LMPT) model was developed to improve the description of hydrogen bonded XH-stretching transitions, where X is typically O or N. We present a modified version of the LMPT model to extend its application from hydrated bimolecular complexes to hydrogen bonded bimolecular complexes with donors such as alcohols, amines and acids. We have applied the modified model to a series of complexes of different hydrogen bond type and complex energy. We found that the differences between local mode (LM) and LMPT calculated fundamental XH-stretching transition wavenumbers and oscillator strengths were correlated with the strength of the hydrogen bond. Overall, we have found that the LMPT model in most cases predicts transition wavenumbers within 20 cm−1 of the experimental values.

AB - The local mode perturbation theory (LMPT) model was developed to improve the description of hydrogen bonded XH-stretching transitions, where X is typically O or N. We present a modified version of the LMPT model to extend its application from hydrated bimolecular complexes to hydrogen bonded bimolecular complexes with donors such as alcohols, amines and acids. We have applied the modified model to a series of complexes of different hydrogen bond type and complex energy. We found that the differences between local mode (LM) and LMPT calculated fundamental XH-stretching transition wavenumbers and oscillator strengths were correlated with the strength of the hydrogen bond. Overall, we have found that the LMPT model in most cases predicts transition wavenumbers within 20 cm−1 of the experimental values.

KW - Explicitly correlated coupled cluster

KW - Frequency redshift

KW - Hydrogen bonds

KW - Intensity enhancement

KW - Vibrational spectroscopy

U2 - 10.1016/j.jms.2017.02.005

DO - 10.1016/j.jms.2017.02.005

M3 - Journal article

AN - SCOPUS:85014431668

VL - 334

SP - 1

EP - 9

JO - Journal of Molecular Spectroscopy

JF - Journal of Molecular Spectroscopy

SN - 0022-2852

ER -

ID: 176440864